Detalhe da pesquisa
1.
Discrete domains of gene expression in germinal layers distinguish the development of gyrencephaly.
EMBO J
; 34(14): 1859-74, 2015 Jul 14.
Artigo
Inglês
| MEDLINE | ID: mdl-25916825
2.
The murine model for Hantaan virus-induced lethal disease shows two distinct paths in viral evolutionary trajectory with and without ribavirin treatment.
J Virol
; 87(20): 10997-1007, 2013 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-23903835
3.
Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles.
Am J Hum Genet
; 82(3): 763-71, 2008 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-18304490
4.
Transcriptome sequencing and development of an expression microarray platform for the domestic ferret.
BMC Genomics
; 11: 251, 2010 Apr 19.
Artigo
Inglês
| MEDLINE | ID: mdl-20403183
5.
Course of seasonal influenza A/Brisbane/59/07 H1N1 infection in the ferret.
Virol J
; 7: 149, 2010 Jul 09.
Artigo
Inglês
| MEDLINE | ID: mdl-20618974
6.
Premature ageing in mice expressing defective mitochondrial DNA polymerase.
Nature
; 429(6990): 417-23, 2004 May 27.
Artigo
Inglês
| MEDLINE | ID: mdl-15164064
7.
A segmental maximum a posteriori approach to genome-wide copy number profiling.
Bioinformatics
; 24(6): 751-8, 2008 Mar 15.
Artigo
Inglês
| MEDLINE | ID: mdl-18204059
8.
Somatic mosaicism for copy number variation in differentiated human tissues.
Hum Mutat
; 29(9): 1118-24, 2008 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-18570184
9.
Profiling of copy number variations (CNVs) in healthy individuals from three ethnic groups using a human genome 32 K BAC-clone-based array.
Hum Mutat
; 29(3): 398-408, 2008 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-18058796
10.
Distal 22q11.2 microduplication encompassing the BCR gene.
Am J Med Genet A
; 146A(23): 3075-81, 2008 Dec 01.
Artigo
Inglês
| MEDLINE | ID: mdl-19006218
11.
A patient with 22q11.2 deletion and Opitz syndrome-like phenotype has the same deletion as velocardiofacial patients.
Am J Med Genet A
; 143A(24): 3302-8, 2007 Dec 15.
Artigo
Inglês
| MEDLINE | ID: mdl-18000907
12.
Overlapping phenotype of Wolf-Hirschhorn and Beckwith-Wiedemann syndromes in a girl with der(4)t(4;11)(pter;pter).
Am J Med Genet A
; 143A(15): 1760-6, 2007 Aug 01.
Artigo
Inglês
| MEDLINE | ID: mdl-17603794
13.
Growth hormone overexpression in the central nervous system results in hyperphagia-induced obesity associated with insulin resistance and dyslipidemia.
Diabetes
; 54(1): 51-62, 2005 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-15616010
14.
NF2 tumor suppressor gene: a comprehensive and efficient detection of somatic mutations by denaturing HPLC and microarray-CGH.
Neuromolecular Med
; 3(1): 41-52, 2003.
Artigo
Inglês
| MEDLINE | ID: mdl-12665675
15.
High-resolution profiling of an 11 Mb segment of human chromosome 22 in sporadic schwannoma using array-CGH.
Int J Oncol
; 22(3): 615-22, 2003 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-12579316
16.
De-novo transcriptome sequencing of a normalized cDNA pool from influenza infected ferrets.
PLoS One
; 7(5): e37104, 2012.
Artigo
Inglês
| MEDLINE | ID: mdl-22606336
17.
Host gene expression signatures discriminate between ferrets infected with genetically similar H1N1 strains.
PLoS One
; 7(7): e40743, 2012.
Artigo
Inglês
| MEDLINE | ID: mdl-22808249
18.
Identification of novel spinal cholinergic genetic subtypes disclose Chodl and Pitx2 as markers for fast motor neurons and partition cells.
J Comp Neurol
; 518(12): 2284-304, 2010 Jun 15.
Artigo
Inglês
| MEDLINE | ID: mdl-20437528
19.
Recurrent genomic alterations in benign and malignant pheochromocytomas and paragangliomas revealed by whole-genome array comparative genomic hybridization analysis.
Endocr Relat Cancer
; 17(3): 561-79, 2010 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-20410162
20.
Frequent genetic differences between matched primary and metastatic breast cancer provide an approach to identification of biomarkers for disease progression.
Eur J Hum Genet
; 18(5): 560-8, 2010 May.
Artigo
Inglês
| MEDLINE | ID: mdl-20051991